CHEMICAL BONDING-4only one mobile electron per atom where as iron has 8 mobile electrons per atom....
Transcript of CHEMICAL BONDING-4only one mobile electron per atom where as iron has 8 mobile electrons per atom....
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Chemical Bonding-IV
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SOLUTION OF CHEMICAL BONDING
CHEMICAL BONDING-4
EXERCISE # 1
PART–I (Hkkx–I)
A-1. (a) Hydrogen molecule (H2) : H2 : (1s)2
Its bond order, therefore, is = 12
02
2
NN ab
(b) Cation of hydrogen molecule (H2+) : H2+ : (1s)1 Its bond order, therefore, is = 1/2 (1 – 0) = 1/2
(c) Helium molecule (He2) : He2 : (1s)2 (*1s)2 Its bond order, therefore, is ½(2 – 2) = 0
(d) Lithium molecule (Li2) : (1s)2 (*1s)2 (2s)2 Its bond order, therefore, is 1/2(4 – 2) = 1.
(e) Beryllium (Be2) : (1s)2 (*1s)2 (2s)2 (*2s)2 Its bond order, therefore, is 1/2(4 – 4) = 0.
(f) Boron (B2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p1x = 2p1y) (pz)0 Its bond order, therefore, is 1/2(6 – 4) = 1.
gy % (a) gkbMªkstu v.kq (H2) : H2 : (1s)2
bldk ca/kØe = 12
02
2
NN ab
(b) gkbMªkstu v.kq dk /kuk;u (H2+) : H2+ : (1s)1
bldk ca/kØe = 1/2 (1 – 0) = 1/2
(c) ghfy;e v.kq (He2) : He2 : (1s)2 (*1s)2
bldk ca/kØe ½(2 – 2) = 0
(d) fyfFk;e v.kq (Li2) : (1s)2 (*1s)2 (2s)2
bldk ca/kØe 1/2(4 – 2) = 1.
(e) csjhfy;e (Be2) : (1s)2 (*1s)2 (2s)2 (*2s)2
bldk ca/kØe 1/2(4 – 4) = 0.
(f) cksjkWu (B2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p1x = 2p1y) (pz)0
bldk ca/kØe 1/2(6 – 4) = 1.
A-3. Complex exists as NO+ and [BF4]– . NO+ is isoelectronic with N2 ; so 1s2, *1s2, 2s2, *2s2, 2p2x =
2p2y, 2pz2 , then its bond order is 2
4–10 = 3
gy % ladqy ;kSfxd NO+ vkSj [BF4]– ds :i esa vfLrRo esa jgrk gSA NO+ rFkk N2 lebysDVªkWfud gS] vr% 1s2, *1s2,
2s2, *2s2, 2p2x = 2p2y, 2pz2 , rc bldk ca/k Øe 2
4–10 = 3.
PART–II (Hkkx–II) A-1. The electron density is zero in the nodal plane during the formation of a molecular orbital from atomic
orbitals of the same atom.
gy % leku ijek.kq ds ijek.oh; d{kd ls ,d vkf.od d{kd ds fuekZ.k esa uksMy ry esa bysDVªkWu ?kuRo 'kwU; gksrk gSA
A-4. (A) Bond order of N2+ = 2.5 ; The bond order of O2+ 1/2(10 – 5) = 2.5. (B) Bond order of F2 = 1 ; The bond order of Ne2 = 0. (C) Bond order of O2 = 2 ; The bond order of B2 = 1. (D) Bond order of C2 = 2 ; The bond order of N2 = 3.
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Chemical Bonding-IV
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Sol. (A) N2+ dk ca/k Øe = 2.5 ; O2+ dk ca/k Øe 1/2(10 – 5) = 2.5.
(B) F2 dk ca/k Øe = 1 ; Ne2 dk ca/k Øe = 0.
(C) O2 dk ca/k Øe = 2 ; B2 dk ca/k Øe = 1.
(D) C2 dk ca/k Øe = 2 ; N2 dk ca/k Øe = 3.
A-6. N22– : 1s2 *1s2 2s2 *2s2 2px2 2py2 2pz2 2px1 *2py1.
B.O. N22– = 2
6–10= 2. ; B.O. O2 =
2
6–10 = 2.
NO– isoelectronic with O2 so B.O. = 2
6–10 = 2.
All have same number of electrons (i.e. 16) so isoelectronic.
gy- N22– : 1s2 *1s2 2s2 *2s2 2px2 2py2 2pz2 2px1 *2py1.
N22– dk ca/k Øe = 2
6–10 = 2. ; O2 dk ca/k Øe =
2
6–10 = 2.
NO– , O2 dk lebysDVªkWfud gS] vr% ca/k Øe = 2
6–10 = 2.
lHkh leku la[;k esa bysDVªkWu j[krs gS] (vFkkZr~ 16) vr% lebysDVªkWfud gSaA
B-1. B2 bond order = 1 ; C2 bond order = 2 ; F2 bond order = 1 ; O2– bond order = 1.5
bond order 1/bond length.
B2 ca/k Øe = 1 ; C2 ca/k Øe = 2 ; F2 ca/k Øe = 1 ; O2– ca/k Øe = 1.5
ca/k Øe 1/ca/k yEckbZ
B-2. (A) NO– is derivative of O2 and isoelectronic with O2.
So (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x = 2p2y ) (*2px1 = *2p1y) and 2 unpaired electrons.
(B) O22– : (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x = 2p2y) (*2px2 = *2p2y) and no unpaired electrons.
(C) CN– is derivative of and isoelectronic with N2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2 and no unpaired electron.
(D) CO is derivative of and isoelectronic with N2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2 and no unpaired electron.
gy % (A) NO–, O2 dk O;qRiUu gS rFkk O2 ds lkFk lebysDVªksfud (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x =
2p2y) (*2px1 = *2p1y) vkSj 2 v;qfXer bysDVªkWu gSA
(B) O22– : (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x = 2p2y) (*2px2 = *2p2y) dksbZ v;qfXer bysDVªksu ugha gSA
(C) CN– dk O;qRiUu gS rFkk N2 ds lkFk lebysDVªksfud : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2
vkSj dksbZ v;qfXer bysDVªkWu ugha gSA
(D) CO, N2 dk O;qRiUu ,oa lebysDVªkWfud gS (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2 vkSj dksbZ
v;qfXer bysDVªkWu ugha gSA
B-3. O2 O2– O22– O2+ Bond Order 2 1.5 1 2.5
gy. cU/k Øe O2 O2– O22– O2+
2 1.5 1 2.5
B-5. From MOT & bond order values.
MOT o ca/k Øe ekuks ls
C-1. The strength of metallic bonds depends upon the number of mobile electron(s) per atom. Sodium has only one mobile electron per atom where as iron has 8 mobile electrons per atom.
fdlh Hkh /kkfRod ca/k dh izcyrk bl ckr ij fuHkZj djrh gS fd mlesa izfr ijek.kq xfr'khy bysDVªkWu fdrus gSA Na
esa izfr ijek.kq ek=k ,d rFkk vk;ju esa izfr ijek.kq vkB (8) xfr'khy bysDVªkWu gSaA
C-2. Electron sea model of metallic bonding.
/kkfRod ca/k dk bysDVªkWu leqnz ekWMyA
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Chemical Bonding-IV
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C-3. Cu, Ag, Zn are solids at room temperature where as mercury is liquid.
Cu,Ag, Zn dejs ds rki ij Bksl gS tcfd edZjh nzo gSA
EXERCISE # 2
PART – I (Hkkx - I)
1. (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2 ; number of anti bonding electrons in N2 is 4. * represents antibonding molecular orbitals.
gy % (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2 ; N2 esa izfrca/kh bysDVªkWu dh la[;k 4 gSA
* izfrca/kh vkf.od d{kd dks n'kkZrk gSA
2. B.O. ca/k Øe = 2
410=
2
6 = 3
3. 2e
H = (1s2)(1*s1) B.O. =2
12 =
2
1
2e
H = (1s2)(1*s1) ca/k Øe = 2
12 =
2
1
4. B2 : (1s)2(1s)2(2s)2(2s)2(2Px1 = 2Py1)
B.O. ca/k Øe = 2
45 = 2
1 > 0
Rest all have zero B.O.
ckdh lHkh ds ca/k Øe 0 gSA
5. (A) O2– B.O = 1½ (B) O2 B.O = 2 (C) O2+ = 2½ (D) O22 – = 1
Bond order lengthbond
1 ca/k Øe
Zca/k yEckb
1
6. B.O. lengthBond
1 (ca/k Øe
Zca/k yEckb
1 )
7. NO– > NO > NO+ (bond length) Bond order 2.0 2.5 3 H2 > H2+ > He2+ (bond energy) Bond order 1 0.5 0.5 (In He2+ more electron in antibonding MO's) NO2+ > NO2 > NO2– (bond angle) Bond angle 180º 133º 115º O22– < O2+ < O2 (paramagnetic moment) No. of unpaired e– 0 1 2
gy% NO– > NO > NO+ (ca/k yEckbZ)
ca/k Øe 2.0 2.5 3
H2 > H2+ > He2+ (ca/k ÅtkZ)
ca/k Øe 1 0.5 0.5
(He2+ esa] vkcU/kh MO's esa vf/kd bysDVªkWu gksrs gSA)
NO2+ > NO2 > NO2– (ca/k dks.k)
ca/k dks.k 180º 133º 115º
O22– < O2+ < O2 (vuqpqEcdh; vk?kw.kZ)
v;qfXer bysDVªkWuksa dh la[;k 0 1 2
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Chemical Bonding-IV
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8. He2+ bond order = 2
1
2
12
; O2– bond order = 5.12
710
C2 bond order = 22
48
; NO bond order = 5.22
510
Bond order bond dissociation energy.
gy. He2+ cU/k Øe = 2
1
2
12
; O2– cU/k Øe = 5.12
710
C2 cU/k Øe = 22
48
; NO cU/k Øe = 5.22
510
cU/k Øe cU/k fo;kstu ÅtkZ
9. N2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2 The bond order of N2 is 1/2(10 – 4) = 3.
N2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)1 The bond order of N2+ is 1/2(9 – 4) = 2.5.
O2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px1 = *2p1y) The bond order of O2 1/2(10 – 6) = 2.
O2– : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px2 = *2p1y) The bond order of O2 1/2(10 – 7) = 1.5.
NO+ derivative of O2 and isoelectronic with O22+ ; so (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x = 2p2y) The bond order of NO+ 1/2(10 – 4) = 3.
NO derivative of O2 and isoelectronic with O2+; (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x=2p2y),
*2px)1 The bond order of NO is 1/2(10 – 5) = 2.5.
Bond order 1/bond length bond dissociation energy.
gy % N2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)2
N2 ¼ukbVªkstu½ dk ca/k Øe gS 1/2(10 – 4) = 3.
N2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) 2pz)1
N2+ dk ca/kØe gSA 1/2(9 – 4) = 2.5.
O2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px1 = *2p1y)
vkWDlhtu O2 dk ca/k Øe gSA 1/2(10 – 6) = 2.
O2– : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px2 = *2p1y)
O2 dk ca/k Øe gSA 1/2(10 – 7) = 1.5.
NO+ tks O2 dk O;qRiUu gS vkSj O22+; ls lebysDVªksfud gS] (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x=2p2y)
NO+ dk ca/k Øe gS 1/2(10 – 4) = 3.
NO tks O2 dk O;qRiUu gS rFkk O2+ ; (1s)2 (*1s)2 (2s)2 (*2s)2 2pz)2 (2p2x=2p2y), *2px)1
NO dk ca/k Øe gS is 1/2(10 – 5) = 2.5.
ca/k Øe 1/ca/k yEckbZ ca/k fo;kstu ÅtkZA
10. N2O4
O2–, NO2 and ClO2 are odd electron species. (O2–, NO2 rFkk ClO2 ds ikl v;qfXer e– gSA)
11. Metallic bond results from the electrical attractions among positively charged metal ions and mobile,
delocalised electrons belonging to the crystal as a whole.
gy % /kuvkosf'kr /kkfRod vk;uksa rFkk xfr'khy foLFkkuhd`r bysDVªkWu ds e/; oS|qr vkd"kZ.k ds QyLo:i /kkfRod ca/k
curk gSA
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Chemical Bonding-IV
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PART – II (Hkkx - II)
1. N2+, N2– , O2+, C2+ have fractional bond order.
Sol. N2+, N2– , O2+, C2+ fHkUukRed ca/k dks.k j[krs gSA
PART – III (Hkkx - III) 1. O22+ bond order = 3, NO+ bond order = 3, CN– bond order = 3, CN+ bond order = 2
O22+ ca/k Øe = 3, NO+ ca/k Øe = 3, CN– ca/k Øe = 3, CN+ ca/k Øe = 2
2. (A) ON:.
(B) (C) (D)
3. In FO+ total no. of electrons = 16, so bond order will be 2. In FO– total number of electrons = 18, so bond order will be 1.
gy. FO+ esa dqy bysDVªkWuksa dh la[;k = 16, vr% cU/k Øe 2 gksxkA
FO– esa dqy bysDVªkWuksa dh la[;k 18 gS] vr% cU/k Øe 1 gksxkA
4. (A) O2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px1 = *2py)
(B) NO is derivative of O2: NO(O2+) (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px1 = *2py)
(C) O2– : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px2 = *2p1y)
(D) B2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p1x = 2p1y) (pz)0
gy- (A) O2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px1 = *2py)
(B) NO, O2 dk O;qRiUu gS : NO(O2+) (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px1 = *2py)
(C) O2– : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px2 = *2p1y)
(D) B2 : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p1x = 2p1y) (pz)0
5. Facts rF;A
6. Facts rF;A
7. Facts rF;A
PART – IV (Hkkx - IV)
1. (A)
Bond order stability (i.e., bond strength)
(B) Helium molecule (He2) : He2 : (1s)2 (*1s)2 Bond order of He2 is ½(2 – 2) = 0 The molecular orbital description of He2 predicts two electrons in a bonding orbital and two electrons in
an antibonding orbital, with a bond order of zero - in other words, no bond. The noble gas He has not significant tendency to form diatomic molecules and, like the other noble gases, exists in the form of free atoms.
(C) Carbon molecule (C2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) or KK (2s)2 (*2s)2 (2p2x
= 2p2y )
Lithium molecule (Li2) : (1s)2 (*1s)2 (2s)2
Peroxide (O22–) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px2 = *2p2y) As all electrons are paired so C2, Li2 and O22– are diamagnetic.
(D) Fluorine molecule (F2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px2 = *2p2y)
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Chemical Bonding-IV
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Sol. (A)
vkca/k Øe LFkkf;Ro (vFkkZr~ vkca/k lkeF;Z)
(B) ghfy;e v.kq (He2) : He2 : (1s)2 (*1s)2
He2 dk ca/k Øe ½(2 – 2) = 0 gSaA
He2 v.kq ds vkf.od d{kd o.kZu esa] nks bysDVªkWu ca/kh d{kd esa rFkk nks bysDVªkWu çfrca/kh d{kd esa mifLFkr gSA
bldk caèk Øe 'kwU; gksrk gSA nwljs 'kCnksa esa dksbZ ca/k ugha curk gSaA vU; ukscy xSlksa ds leku vfØ;@ukscy xSl
He Hkh f}ijek.kqd v.kq esa vfLrRo ugha j[krk gSa rFkk ,dy•ijek.kq ds :i esa vfLrRo j[krk gSaA
(C) dkcZu v.kq (C2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y) or KK (2s)2 (*2s)2 (2p2x = 2p2y )
fyfFk;e v.kq (Li2) : (1s)2 (*1s)2 (2s)2
ijvkWDlkbM (O22–) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px2 = *2p2y)
pwafd lHkh bysDVªkWu ;qfXer gS] vr% C2, Li2 rFkk O22– çfrpqEcdh; gSaA
(D) ¶yksjhu v.kq (F2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px2 = *2p2y)
2. (D) It is correct statement. (D) ;g lgh dFku lgh gSaA
3. (B) Oxygen molecule (O2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px1 = *2p1y) Bond order = 1/2(10 – 6) = 2.0,
O2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px1 = *2p0y) Bond order = 1/2(10 – 5) = 2.5.
Nitrogen molecule (N2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y ) 2pz)2 The bond order of N2 is 1/2(10 – 4) = 3.
N2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y ) 2pz)1 Bond order = 1/2(9 – 4) = 2.5.
gy- (B) vkWDlhtu v.kq (O2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y) (*2px1 = *2p1y)
ca/k Øe = 1/2(10 – 6) = 2.0,
O2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px1 = *2p0y)
ca/k Øe = 1/2(10 – 5) = 2.5.
ukbVªkstu v.kq (N2) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y ) 2pz)2
N2 dk ca/k Øe 1/2(10 – 4) = 3 gSaA
N2+ : (1s)2 (*1s)2 (2s)2 (*2s)2 (2p2x = 2p2y ) 2pz)1
ca/k Øe = 1/2(9 – 4) = 2.5.
(9-11). B2 (10 e) 2
1s < 2
*1s < 2
2s < 2
* 2s < 1 1
x y( 2p 2p ) < *2pz.
Nb = 6 e, Na = 4 , B.O. = b aN N
2
=
6 4
2
= 1
And S.P. mixing occurs, Paramagnetic in nature, HOMO is BMO.
(rFkk S.P. lfEeJ.k izkIr gksrk gS] vuqpqEcdh; izd`fr, HOMO, BMO gSA)
2O
(15 e) 2
1s < 2
*1s < 2
2s < 2
* 2s < 2
z2p < 2 2
x y( 2p 2p ) < (1
x* 2p = *2py) < *2pz
Nb = 10 e, Na = 5 , B.O. = b aN N
2
=
10 5
2
= 2.5
And no S.P. mixing occur, Paramagnetic in nature, HOMO is ABMO.
(rFkk S.P. lfEeJ.k izkIr ugha gksrk gS] vuqpqEcdh; izd`fr, HOMO, ABMO gSA)
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Chemical Bonding-IV
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F2 (18 e) 2
1s < 2
*1s < 2
2s < 2
* 2s < 2
z2p < 2 2
x y( 2p 2p ) < (2
x* 2p = 2
y* 2p ) < *2pz
Nb = 10 e, Na = 8 , B.O. = b aN N
2
=
10 8
2
= 1
And no S.P. mixing occur, Diamagnetic in nature, HOMO is ABMO
(rFkk S.P. lfEeJ.k izkIr gksrk gS] izfrpqEcdh; izd`fr, HOMO, ABMO gSA)
C2 (12 e) 2
1s < 2
*1s < 2
2s < 2
* 2s < 2 2
x y( 2p 2p ) < *2pz.
Nb = 8 e, Na = 4 , B.O. = b aN N
2
=
8 4
2
= 2
And S.P. mixing occur, Diamagnetic in nature, HOMO is BMO.
(rFkk S.P. lfEeJ.k izkIr gksrk gS] izfrpqEcdh; izd`fr, HOMO, BMO gSA)
EXERCISE # 3
PART – I (Hkkx - I)
2. O2– is derivative of O2 and has 17 electrons. So its molecular orbital electronic configuration is
21s 21* s 22s 22* s 22 zp 2
2 xp 2
2 yp 2
2*
xp 1
2*
yp
As it contains one unpaired electron in *2py1 molecular orbital so it is paramagnetic. Rest all species
have paired electrons so diamagnetic.
gy- O2– , O2 dk O;qRiUu gksrk gS o 17 e
– j[krk gSA blfy, bldk v.kq d{kd bysDVªkWfud foU;kl gSaA
21s 21* s 22s 22* s 22 zp 2
2 xp 2
2 yp 2
2*
xp 1
2*
yp
pawfd ;g *2py1 v.kqd{kd esa ,d v;qfXer bysDVªkWu j[krk gS blfy, ;g vuqpqEcdh; gksrk gSA ckdh lHkh ;qfXer
bysDVªkWu j[krs gS blfy, izfrpqEcdh; gksrs gSA
3. Molecular orbital electronic configuration is 21s 21* s 22s 22* s 22 zp 2
2 xp 2
2 yp 1
2*
xp 0
2*
yp
As it contains one unpaired electron it is paramagnetic and bond order = (10 – 5) / 2 = 2.5 (O2 = 2.0).
gy- vkf.od d{kd bysDVªkWfud foU;kl 21s 21* s 22s 22* s 22 zp 2
2 xp 2
2 yp 1
2*
xp 0
2*
yp gSA
blesa ,d v;qfXer bysDVªkWu gksrk gSA vr% ;g vuqpqEcdh; gS vkSj cU/k Øe = (10 – 5) / 2 = 2.5 (O2 = 2.0).
5. Bond order = b aN –N
2
CO = 21s 21s* 22s 22s* 2x2p 2
y2p 2
z2p
Bond order of CO = 10 – 4 / 2 = 3
NO– 21s 21s* 22s 22s* 2z2p 2
x2p 2
y2p 1
x2p* 1
y2p*
Bond order of NO– = 10 – 6 / 2 = 2
NO+ 21s 21s* 22s 22s* 2z2p 2
x2p 2
y2p
Bond order of NO+ = 10 – 4 / 2 = 3
CN– 21s 21s* 22s 22s* 2x2p 2
y2p 2
z2p
Bond order of CN– = 10 – 4 / 2 = 3
N2 21s 21s* 22s 22s* 2x2p 2
y2p 2
z2p
Bond order of N2 = 10 – 4 / 2 = 3.
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Chemical Bonding-IV
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gy- cU/k Øe = b aN –N
2
CO = 21s 21s* 22s 22s* 2x2p 2
y2p 2
z2p
CO esa cU/k Øe = 10 – 4 / 2 = 3
NO– 21s 21s* 22s 22s* 2z2p 2
x2p 2
y2p 1
x2p* 1
y2p*
NO– esa cU/k Øe = 10 – 6 / 2 = 2
NO+ 21s 21s* 22s 22s* 2z2p 2
x2p 2
y2p
NO+ esa cU/k Øe = 10 – 4 / 2 = 3
CN– 21s 21s* 22s 22s* 2x2p 2
y2p 2
z2p
CN– esa cU/k Øe = 10 – 4 / 2 = 3
N2 21s 21s* 22s 22s* 2x2p 2
y2p 2
z2p
N2 esa cU/k Øe = 10 – 4 / 2 = 3
6. KO2 exists as K+ & O2– . In O2–, superoxide ion there are total number of electrons = 16 + 1 = 17.
MOT configuration = 21s 21s* 22s 22s* 2z2p 2
x2p 2
y2p 2
x2p* 1
y2p*
O2– has one unpaired electron in antibonding *2py1 . So it is paramagnetic.
gy- KO2 , K+ & O2– esa jgrk gSA
O2–, lqij vkWDlkbM vk;u esa] dqy bysDVªkWu la[;k = 16 + 1 = 17.
vkf.od d{kd vfHkfoU;kl = 21s 21s* 22s 22s* 2z2p 2
x2p 2
y2p 2
x2p* 1
y2p*
O2– ds izfrcU/kh vkf.od d{kd *2py1 esa ,d v;qfXer bysDVªkWu gSA vr% ;g vuqpqEcdh; gSA
7. Statement-1 : Germanium is a semiconductor, where the energy gap between adjacent bands is
sufficiently small for thermal energy to be able to promote a small number of electrons from the full valence band to the empty conduction band. This leaves both bands partially filled, so the material can conduct electricity.
Statement-2 : Incorrect statement.
gy- oDrO;-1 : teksZfu;e ,d v)Zpkyd gS] ftles nks lehiorhZ cS.M ds e/; ÅtkZ vUrjky ml rkih; ÅtkZ dh rqyuk
esa] i;kZIr NksVk gksrk gS tks fd dqN la[;k esa bysDVªkWu dks] iw.kZ iwfjr la;kstdrk cS.M ls] fjDr pkydrk cS.M esa
LFkkukUrfjr dj ldrh gSA bl izdkj nksuksa cS.M vkaf'kd :i ls Hkjs gksrs gS] vr% inkFkZ fo|qr dk pkyu djrk gSA
oDrO;-2 : dFku lgh ugha gSA
8. Due to small size of B, it is very difficult to remove the electrons from boron to form ionic bond as it will
require very high energy. On the other hand, due to its very small size having high polarising power causes greater polarisation and eventually significant covalent character according to Fajan's rule.
gy- B ds NksVs vkdkj ds dkj.k] vk;fud ca/k dk fuekZ.k ds fy, cksjksu ls rhu bySDVªkWu fudkyuk vf/kd dfBu gksrk gS]
D;ksafd blds fy, vf/kd ÅtkZ dh vko';drk gksrh gSA nwljs 'kCnksa esa] blds cgqr NksVs vkdkj ds dkj.k] ;g mPp
/kqzo.k {kerk j[krk gSA bl dkj.k ;g cgqr vf/kd /kzqo.krk mRiUu djrk gS] vr% QkW;ku fu;e ds vuqlkj] blesa
lgla;kstd xq.k ik;k tkrk gSA
9. (A) B2 1s2 *1s 2 2s 2 *2s 2 2px1 = 2py1
Bond order = 6 4
2
= 1 Paramagnetic with two unpaired electrons.
It undergoes oxidation as well as reduction which can be explained by taking the following reactions.
2B + 3Cl2 2BCl3 ; 2B + 3Ca Ca3B2 (boride) Mixing of 's' and 'p' orbitals takes place.
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Chemical Bonding-IV
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(B) N2 1s2 *1s 2 2s 2 *2s 2 2px2 = 2py2 2pz2
Bond order = 10 4
2
= 3 Diamagnetic
It undergoes oxidation as well as reduction which can be explained by taking the following reactions.
N2 + O2 2NO ; 6Li + N2 2Li3N Mixing of 's' and 'p' orbitals takes place.
(C) O2– 1s2 *1s 2 2s 2 *2s 2 2pz2 2px2 = 2px 2 *2px2 = *2py1
Bond order = 10 7
2
= 1.5 Paramagnetic with one unpaired electron.
It undergoes oxidation as well as reduction which can be explained by taking the following reactions.
O2– O2 + e– ; O2– + e– O22– Mixing of 's' and 'p' orbitals does not take place.
(D) O2 1s2 *1s 2 2s 2 *2s 2 2pz2 2px2 = 2px2 *2px1 = *2py1
Bond order = 10 6
2
= 2 Paramagnetic with two unpaired electrons.
It undergoes oxidation as well as reduction which can be explained by taking the following reactions.
O2 O2+ + e– ; O2 + e– O2– Mixing of 's' and 'p' orbitals does not take place.
Sol. (A) B2 1s2 *1s 2 2s 2 *2s 2 2px1 = 2py1
vkcU/k Øe = 6 4
2
= 1 nks v;qfXer bysDVªkWu ds lkFk vuqpqEcdh;
bldk vkWDlhdj.k rFkk vip;u gksrk gS tks fd fuEu vfHkfØ;k }kjk le>k;k tk ldrk gSA
2B + 3Cl2 2BCl3 ; 2B + 3Ca Ca3B2 (boride)
blesa 's' rFkk 'p' d{kdks dk feJ.k gksrk gSA
(B) N2 1s2 *1s 2 2s 2 *2s 2 2px2 = 2py2 2pz2
vkcU/k Øe = 10 4
2
= 3 izfrpqEcdh;
bldk vkWDlhdj.k rFkk vip;u gksrk gS tks fd fuEu vfHkfØ;k }kjk le>k;k tk ldrk gSA
N2 + O2 2NO ; 6Li + N2 2Li3N
blesa 's' rFkk 'p' d{kdks dk feJ.k gksrk gSA
(C) O2– 1s2 *1s 2 2s 2 *2s 2 2pz2 2px2 = 2px 2 *2px2 = *2py1
vkcU/k Øe = 10 7
2
= 1.5 ,d v;qfXer bysDVªkWu ds lkFk vuqpqEcdh;
bldk vkWDlhdj.k] vip;u gksrk gS tks fd fuEu vfHkfØ;k }kjk le>k;k tk ldrk gSA
O2– O2 + e– ; O2– + e– O22–
blesa 's' rFkk 'p' d{kdks dk feJ.k ugha gksrk gSA
(D) O2 1s2 *1s 2 2s 2 *2s 2 2pz2 2px2 = 2px2 *2px1 = *2py1
vkcU/k Øe = 10 6
2
= 2 nks v;qfXer bysDVªkWu ds lkFk vuqpqEcdh;A
bldk vkWDlhdj.k] vip;u gksrk gS tks fd fuEu vfHkfØ;k }kjk le>k;k tk ldrk gSA
O2 O2+ + e– ; O2 + e– O2–
blesa 's' rFkk 'p' d{kdks dk feJ.k ugha gksrk gSA
10. B2 ; total number of electrons = 10. The MOT electron configuration violating the Hund's rule will be
thus:
2
1s2
1s*2
2s2
2s* x2
2p y0
2p z0
2p
So, bond order = 6 4
2
= 1
As all electrons are paired, the molecule is diamagnetic.
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Chemical Bonding-IV
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Sol. B2 ; dqy bysDVªksuksa dh la[;k = 10. MOT ds vuqlkj bysDVªksfud foU;kl tks gq.M fu;e dk ikyu ugha djrk og gS
2
1s2
1s*2
2s2
2s* x2
2p y0
2p z0
2p
vr%] ca/k Øe = 6 4
2
= 1
D;ksafd lHkh bysDVªksu ;qfXer gSa vr% v.kq izfrpqEcdh; gSA
11. If 2s-2p mixing is not operative, the increasing order of Molecular orbitals will be :
1s2, *1s2, 2s2, *2s2, 1
2 yx 1
z
2p2P
2p
Considering this Be2 & B2 become diamagnetic, so does N2. Only C2 would be paramagnatic with electronic configuration as above
gy ;fn 2s-2p feJ.k fØ;kfUor ugha gksrk gS] rks vk.kfod d{kdksa dk vkjksgh Øe fuEu gksxk %
1s2, *1s2, 2s2, *2s2, 1
2 yx 1
z
2p2P
2p
Be2 o B2 izfrpqEcdh; gS] ,slk gh N2 ds lkFk gksrk gSA dsoy mijksDr bysDVªkWfud foU;kl ds lkFk C2 vuqpqEcdh;
gksxkA
12. It is d–d axial overlap in same phase, so d–d bonding.
It is p & d lateral overlap in same phase, so it is p–d bonding.
It is p and d lateral overlap in opposite phase, so it is p–d antibonding.
It is d–d axial overlap in opposite phase, so it is d–d antibonding.
gy. ;g leku izkoLFkk esa d–d v{kh; vfrO;kiu j[krs gS] blfy, d–d cU/ku j[krs gSA
;g leku izkoLFkk esa p o d leikf'oZd vfrO;kiu j[krs gS] blfy, p–d cU/ku j[krs gSA
;g foijhr izkoLFkk esa p o d leikf'koZd vfro;kiu j[krs gS] blfy, p–d izfrcfU/kr j[krs gSA
;g foijhr izkoLFkk esa d–d v{kh; vfrO;kiu j[krs gS blfy, ;g d–d izfrcfU/kr j[krs gSA
13.* (A) 22C Total no. of electrons = 14 so it is diamagnetic
(B) 22O Bond order = 3; 2O Bond order = 2
Bond length in 22O is less than bond length in O2.
(C ) Bond order of 2N = 2.5
Bond order of 2He = 1/2
Some energy is released during the formation of 2He from two isolated He atoms.
Sol. (A) 22C bysDVªkWuksa dh dqy la[;k = 14 blfy, ;g izfrpqEcdh; gSA
(B) 22O cU/k Øe = 3; 2O cU/k Øe = 2
22O esa ca/k yEckbZ O2 dh rqyuk esa de gksrh gSA
(C ) 2N dk cU/k Øe = 2.5
2He dk cU/k Øe = 1/2
nks He ijek.kqvksa ls 2He ds fuekZ.k ds nkSjku dqN ÅtkZ eqDr gksrh gSA
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Chemical Bonding-IV
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PART – II (Hkkx - II) JEE(MAIN) OFFLINE PROBLEMS
1. O2 bond order = 2 ; O2– bond order = 1.5 ; O22– bond order = 1.0 ; O2+ bond order = 2.5.
gy- O2 dk ca/k Øe = 2 ; O2– dk ca/k Øe = 1.5 ; O22– dk ca/k Øe = 1.0 ; O2+ dk ca/k Øe = 2.5.
2. NO and NO+ are derivative of O2.
NO(isoelectronic with O2+) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px1 = *2py) Bond order = 1/2(10 – 5) = 2.5.
NO+(isoelectronic with O22+) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px = *2py) Bond order = 1/2(10 – 4) = 3.
Bond order 1/bond length. So NO+ has shorter bond length.
gy % NO rFkk NO+ nksuksa O2 O;qRiUu gSA
NO (O2+ ls lebysDVªkWfud) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px1 = *2py)
ca/k Øe = 1/2(10 – 5) = 2.5.
NO+(O22+ ls lebysDVªkWfud) : (1s)2 (*1s)2 (2s)2 (*2s)2 (2pz)2 (2p2x = 2p2y ) (*2px = *2py)
ca/k Øe = 1/2(10 – 4) = 3.
ca/k Øe 1/ca/k yEckbZ
blfy, NO+ esa NksVh ca/k yEckbZ gksrh gSaA
3. He2+ (1s)2, *(1s)1, one unpaired electron.
H2 (1s)2 , *(1s)0 , no unpaired electron.
H2+ (1s)1, *(1s)0, one unpaired electron.
H2– (1s)2, *(1s)1, one unpaired electron.
Sol. He2+ (1s)2, *(1s)1, ,d v;qfXer bysDVªkWuA
H2 (1s)2, *(1s)0 , dksbZ Hkh v;qfXer bysDVªkWu ugha gSA
H2+ (1s)1, *(1s)0, ,d v;qfXer bysDVªkWu gSA
H2– (1s)2, *(1s)1, ,d v;qfXer bysDVªkWu gSA
4. The electronic configuration of oxygen atom is 1s2, 2s2, 2p4. Each oxygen atom has 8 electrons. Hence in each O22– ion there are 16 + 2 = 18 electrons. The electronic configuration of O22– ion is
KK (2s)2 * (2s)2 (2pz)2 (2px) p (2py)2*(2px)2 * (2py)2 Here KK represents non-bonding molecular orbital of 1s orbital. O22– contains no unpaired electrons. The electronic configuration of B2 molecule is
KK (2s)2 *(2s)2 (2px)1 (2pz)1 it contains 2 unpaired electrons. The electronic configuration of N2+ ion is
KK (2s)2 *(2s)2 (2px)2 (2py)2 (2pz)1 it contains one unpaired electron. The electronic configuration of O2 molecule is
KK (2s)2 *(2s)2 (2px)2 (2py)2 (2pz)2 *(2px)1 *(2py)1 It contains 2 unpaired electron.
Sol. vkWDlhtu ijek.kq dk bysDVªkWfud foU;kl 1s2, 2s2, 2p4 gSA çR;sd vkWDlhtu ijek.kq ds ikl 8 bysDVªkWu gSA
vFkkZr~ O22– ds ikl 16 +2 = 18 bysDVªkWu gSA O22– vk;u dk bysDVªkWfud vfHkfoU;kl gSA
KK (2s)2 * (2s)2 (2pz)2 (2px) p (2py)2*(2px)2 * (2py)2
tgk¡ KK, 1s d{kd ds foijhr ca/kh vkf.od d{kdksa dks n'kkZrk gSA O22– esa dksbZ Hkh v;qfXer bysDVªkWu ugha gSA
B2 v.kq dk bysDVªkWfud foU;kl
KK (2s)2 *(2s)2 (2px)1 (2pz)1
;g 2 v;qfXer bysDVªkWu j[krk gSA N2+ vk;u dk bysDVªkWfud foU;kl
KK (2s)2 *(2s)2 (2px)2 (2py)2 (2pz)1
;g ,d v;qfXer bysDVªkWu j[krk gSA
O2 v.kq dk bysDVªkWfud foU;kl
KK (2s)2 *(2s)2 (2px)2 (2py)2 (2pz)2 *(2px)1 *(2py)1
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Chemical Bonding-IV
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;g 2 v;qfXer bysDVªkWu j[krk gSA
5. O22– (8 + 8 + 2 = 18) : 1s2 *1s2 2s2 *2s2 2pz2 2px2 2py2 *2px2 *2py2 ;
all electrons are paired. So diamagnetic. (lHkh bysDVªkWu ;qfXer gSA vr% çfrpqEcdh; gSA)
6. Molecular orbital configuration of
vkf.od d{kd dk foU;kl
O2 1s2* 1s2 2s2 *2s2 2pz2 2py2 *2p1x *2p1y
Paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 10 – 6
2 = 2
O2+ 1s2* 1s 2s2* 2s2 2p2z 2px2 2py2 * 2p1x
Paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 10 – 5
2= 2.5
N2 1s2* 1s2 2s2 *2s2 2p2x 2p2y 2p2z
paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 10 – 4
2= 3
N2+ 1s2 * 1s2 2s2 * 2s2 2p2x 2p2y 2p1z
Paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 9 – 4
2 = 2.5
C2 1s2 * 1s2 2s2 * 2s2 2p2x 2p1y
Paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 8 – 4
2 = 2
C2+ 1s2 * 1s2 2s2 * 2s2 2p2x 2p1y
Paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 7 – 4
2 = 1.5
NO 1s2 * 1s2 2s2 * 2s2 2p2z 2p2x 2p2y * 2p1x
Paramagnetic vuqpqEcdh;
ca/k dksfV Bond order = 10 – 5
2 = 2.5
NO+ 1s2 * 1s2 2s2 * 2s2 2p2z 2p2x 2p2y
Diamagnetic çfrpqEcdh;
ca/k dksfV Bond order = 10 – 4
2 = 3.
7. NO+ is derivative of O2 ; NO+ (isoelectronic with O22+) 1s2 * 1s2 2s2 * 2s2 2p2z 2p2x 2p2y
Bond order = 10 – 4
2= 3.
CN– is derivative of N2 ; CN– (isoelectronic with N2) 1s2 * 1s2 2s2 * 2s2 2p2x 2p2y 2p2z
Bond order = 10 – 4
2= 3.
NO+ , O2 dk O;qRiUu gS ; NO+ ( O22+ ds lkFk lebysDVªkWfud gS) 1s2 * 1s2 2s2 * 2s2 2p2z 2p2x 2p2y
ca/k Øe = 10 – 4
2 = 3.
CN– , N2 dk O;qRiUu gS ; CN– (N2 ds lkFk lebysDVªkWfud gS) 1s2 * 1s2 2s2 * 2s2 2p2x 2p2y 2p2z
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Chemical Bonding-IV
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ca/k Øe = 10 – 4
2 = 3.
8. Bond Order (cU/k Øe)
(1) O2+ 10 5
2
= 2.5
(2) O2– 10 7
2
= 1.5
(3) O22– 10 8
2
= 1
(4) O22+ 10 4
2
= 3
Bond order 1
bond length (cU/k Øe
1
cU/k yEckbZ)
So, O22+ has the shortest bond length. vr%] O22+ dh cU/k yEckbZ lcls de gksxhA
9.* N2 and C2 both are diamagnetic Ans is (1) and (2)
N2 rFkk C2 nksuksa izfrpqEcdh; gSA
vr% mRrj (1) vkSj (2) gksxkA
10. H22+ : Bond order = 0
He2 : Bond order = 2 2
02
So, both H22+ & He2 do not exist.
gy- H22+ : ca/k Øe = 0
He2 : ca/k Øe = 2 2
02
vr%] H22+ rFkk He2 nksuksa vfLrRo ugha j[krs gSA
11. Li2 1s2 1s2 2s2 Bond order = 1
Li2+ 1s2 1s2 2s1 Bond order = 0.5
Li2– 1s2 1s2 2s2 2s1 Bond order = 0.5 Stability order Li2 > Li2+ > Li2–
Sol. Li2 1s2 1s2 2s2 ca/k Øe = 1
Li2+ 1s2 1s2 2s1 ca/k Øe = 0.5
Li2– 1s2 1s2 2s2 2s1 ca/k Øe = 0.5
LFkkf;Ro dk Øe Li2 > Li2+ > Li2–
12. No of electron in CO = 6 + 8 = 14
(i) CO 1S2, *1S2, 2S2,* 2S2,
2 2 2x y Z2P 2P 2P
All electrons are paired so diamagnetic
(ii) O2 1S2, *1S2, 2S2, * 2S2, 2PZ2 2 2 * 1 * 1x y x y2P 2P , 2P 2P
Unpaired electron = 2 (Paramagnetic)
(iii) B2 1S2, *1S2, 2S2, *2S2 1 1x y2P 2P (Paramagnetic)
(iv) NO 1S2,*1S2, 2S2, *2S2, 2PZ2 * *2 2 1 0
x y x y2P 2P , 2P 2P
(Paramagnetic)
Sol. CO esa bysDVªksuks dh la[;k = 6 + 8 = 14
(i) CO 1S2, *1S2, 2S2, *2S2, 2 2 2x y Z2P 2P 2P
lHkh bysDVªkWu ;qfXer gSA vr% izfrpqEcdh; gSA
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Chemical Bonding-IV
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(ii) O2 1S2, *1S2, 2S2, *2S2, 2PZ2 2 2 * 1 * 1x y x y2P 2P , 2P 2P
v;qfXer bysDVªkWu = 2 (vuqpqEcdh;)
(iii) B2 1S2, *1S2, 2S2, *2S2 1 1x y2P 2P (vuqpqEcdh;)
(iv) NO 1S2, *1S2, 2S2, * 2S2, 2PZ2 * *2 2 1 0
x y x y2P 2P , 2P 2P
(vuqpqEcdh;)
13. H22– have bond order zero do not exist
H22– 'kqU; cU/k Øe j[krk gSA vr% vfLrRo ugh gSA
H22–1S2, *1S2, B.O. = 2 – 2
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JEE(MAIN) ONLINE PROBLEMS
4. Bonding molecular orbital results in increased electron density between nuclei due to constructive interference of combining electron waves.
Sol. la;ksth bysDVªkWu rjaxksa dk leiks"kh; O;frdj.k ds dkj.k ca/kh vkf.od d{kd (MO) esa] ukfHkdksa ds e/; bysDVªkWu
?kuRo c